Freelance Clinical Project Manager Vaccines Latam

K-Recruiting Life Sciences; Teletrabalho; BRL 80.000 - 120.000; Tempo integral

Resumo da oferta

A leading life sciences recruitment company is seeking an experienced Project Manager to oversee clinical projects. This remote position requires a strong background in regulatory and project management practices. Applicants should have over three years of cross-functional clinical experience, proficient communication skills, and the ability to lead diverse teams. Responsibilities include planning and executing projects on time and within budget while ensuring compliance with regulatory standards. The role is expected to start in December 2025 and lasts for 12 months.

Qualificações

• 3+ years cross‑functional clinical PM experience.
• Strong knowledge of regulatory / GEP and RA / MOH requirements.
• Ability to interpret protocols across regions.
• Experience in end-to-end project delivery and risk management.
• Proficiency in study plan development and PM tools.
• Experience in budget forecasting and scope control.
• Clear communication skills for stakeholder engagement.
• Adaptable and solution-oriented with a proactive approach.

Responsabilidades

• Ensure regulatory and GxP / GEP compliance.
• Plan, execute, and close clinical projects within scope, time, and budget.
• Oversee budget forecasting and burn rate monitoring.
• Lead cross‑functional teams and foster collaboration.
• Communicate clearly with sponsors, vendors, and stakeholders.
• Anticipate issues and develop mitigation strategies.

Conhecimentos

Cross‑functional clinical PM experience

Regulatory / GEP and RA / MOH knowledge

Protocol interpretation

Risk, resource & milestone management

Study plan development

Budget forecasting

Stakeholder communication

Adaptability & solution-oriented approach

Descrição da oferta de emprego

Tasks

Ensure regulatory and GxP / GEP compliance; strong understanding of RA / MOH requirements and protocol implementation across regions.

Plan, execute, and close clinical projects within scope, time, and budget; build timelines and manage risks, resources, and milestones.

Oversee budget forecasting, burn rate monitoring, and scope change control.

Lead cross‑functional teams (Clinical, Epi, DM, Stats, Reg, PVG) and foster collaboration and accountability.

Communicate clearly with sponsors, vendors, and stakeholders; translate complex requirements into actionable steps.

Anticipate issues, develop mitigation strategies, and adapt to regulatory or operational changes.

Qualifications

• 3+ years cross‑functional clinical PM experience
• Strong regulatory / GEP and RA / MOH knowledge
• Protocol interpretation across regions
• End‑to‑end project delivery; risk, resource & milestone management
• Study plan development; proficient with PM tools
• Budget forecasting, burn‑rate & scope control
• Clear stakeholder communication & actionable guidance
• Risk anticipation, adaptability & solution‑oriented approach

Requirements

Start: 12/2025

Duration: 12 months

Capacity: 4 days per week

Location: remote